Bur oak blight, a new disease on Quercus macrocarpa caused by Tubakia iowensis sp. nov.

A newly recognized, late-season leaf disease of Quercus macrocarpa (bur oak) has become increasingly severe across Iowa and in neighboring states since the 1990s. Vein necrosis and leaf death may occur over the whole crown or only on the lower branches. Symptoms typically intensify year-to-year in individual trees, and there appears to be substantial variation in susceptibility. Distinctive conidiomata (pycnothyria with a shield of radiating, setae-like hyphae) of a Tubakia sp. are found along the necrotic leaf veins. The same species produces a second type of pycnothyrium with a crustose covering and smaller conidia on the petioles of killed leaves, which remain on the tree through the winter and provide the primary inoculum to infect newly emerging shoots and leaves in spring. Comparison of the Tubakia sp. on bur oak with T. dryina and other species of Tubakia led to the conclusion that the species on bur oak is new, distinct from T. dryina, which herein is defined more narrowly. Inoculation studies confirmed that Tubakia iowensis sp. nov. is the cause of bur oak blight. Bur oak blight appears to be particularly severe on Q. macrocarpa var. oliviformis, which is well adapted to the dry, upland sites where the disease is found most frequently. The recent climatic trend in Iowa to higher spring precipitation might have led to increased severity of the disease.

Phylogenetic and taxonomic evaluation of Chalara, Chalaropsis, and Thielaviopsis anamorphs associated with Ceratocystis.

Parsimony analysis of sequences of the internal transcribed spacer region of the nuclear rDNA and partial sequences of the large subunit (LSU) place four anamorphic Chalara species as a monophyletic grouping within the teleomorph genus Ceratocystis. Chalara ovoidea, Ch. thielavioides, Ch. populi, and Ch. elegans (synanamorph: Thielaviopsis basicola) form aleurioconidia typical of the anamorph genus Thielaviopsis, to which the species are transferred. Three of these species (T. ovoidea, T. thielavioides, and T. populi) are morphologically similar to each other but are shown to be distinct by rDNA sequences. The anamorphic genera Chalaropsis and Hughesiella are considered synonyms of Thielaviopsis. Thielaviopsis punctulata, which forms aleurioconidia singly, is shown to be the anamorph of Ce. radicicola. The respective anamorphs for Ce. coerulescens, Ce. fagacearum, and Ce. eucalypti, which lack aleurioconidia, are also transferred to the amended genus Thielaviopsis as T. ungeri, T. quercina, and T. eucalypti. Although Ch. australis and Ch. neocaledoniae do not form aleurioconidia, they are placed in Thielaviopsis based on their endoconidial state and clear affinities to Ceratocystis eucalypti. Three apparently asexual Ambrosiella species belong in the Ce. moniliformis clade based on LSU rDNA sequences, but the cultures available are not suitable for detailed morphological study, and these species are not transferred to Thielaviopsis.

Epitypification of Ophiostoma galeiforme and phylogeny of species in the O. galeiforme complex.

Ophiostoma galeiforme was described first in 1951 from Larix kaempferi in Scotland, where it was found to be associated with the bark beetles Hy-lurgops palliatus, Dryocoetes autographus, and the ambrosia beetle Trypodendron lineatum. The taxonomy of this fungus has been uncertain because of a lack of sexual structures on the type specimen and contamination of a preserved ex-type culture. The aim of this study was to clarify application of the species name, O. galeiforme, by designating an epitype and to consider phylogenetic relationships of the species. Nineteen isolates resembling O. galeiforme from different parts of the world were used, including collections from Pinus sylvestris infested with Tomicus pi-niperda in Scotland and the contaminated ex-type culture. Morphological characteristics of isolates from Sweden, South Africa, Scotland, Chile and Aus-tria corresponded well with those originally described for O. galeiforme, and an isolate from Scotland is designated as the epitype. A detailed description is provided. Results of interfertility tests showed that O. galeiforme is heterothallic. Analysis of ITS rDNA sequences showed that the isolates representing O. galeiforme were distinct from three morphologically similar isolates from the USA and Mexico, which probably represent an undescribed taxon.